Canonical Allele Identifier: PA2828327411
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro300Leu
CA232923
NM_001369393.2:c.899C>T